ODCs

Click node...

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Partial atrioventricular canal

Atrial septal defect - atrioventricular conduction defects

CRELD1	(UniProt - OMIM)		NKX2-5	(UniProt - OMIM)
GATA4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GATA4	(0.96)	NKX2-5

Citations in the biomedical literature:

Partial atrioventricular canal		Atrial septal defect - atrioventricular conduction defects

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare surgical cardiac disease		Classification (Orphanet): - Rare cardiac disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: C536112		External references: 1 OMIM reference - No MeSH references

Atrial septal defect - atrioventricular conduction defects
	Very frequent - Autosomal dominant inheritance - Cardiac conduction defect / sinoauricular / heart / auriculoventricular / branch block - Cardiac septal defect
Partial atrioventricular canal
(no data available)